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Biphasic Calcium Phosphate vs. Hydroxyapatite in Sinus Floor Elevation

Sinus Floor Augmentation Clinical Trial

Official title:
Sinus Augmentation Using Symbios Versus Algipore as Bone Graft Material - A Randomized Controlled Clinical Pilot Study

Clinical Trial Summary

Twenty patients scheduled for lateral-window sinus floor Elevation (SFE) are randomized into two groups: use of SYMBIOS® Biphasic Bone Graft Material (Group 1) or of Algipore® Bone Substitution Material (Group 2).

Biopsies are taken 3 months after SFE and during implant surgery after 6 months. One ground section per biopsy (n=40) is stained, scanned, and histomorphometrically analyzed for new bone, old bone, soft tissue, graft, bone infiltration of graft, bone-to-graft contact, and penetration depth.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04331314
Study type Interventional
Source Medical University of Graz
Contact
Status Completed
Phase N/A
Start date February 23, 2015
Completion date October 28, 2019
View Details
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